Prednisolone
- Product NDC
- 70518-2084
- 11-digit product format
- 705182084
- Labeler code
- 70518
- Product ID
- 70518-2084_8909cfeb-e92a-82b5-e053-2995a90a71b8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisolone
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA040401
- Marketing category
- ANDA
- Marketing start
- 2019-05-15
- Marketing end
- 0000-00-00
- Substance
- PREDNISOLONE
- Active strength
- 15 mg/5mL
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record